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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:SETD2-MRPL44 (FusionGDB2 ID:80317)

Fusion Gene Summary for SETD2-MRPL44

check button Fusion gene summary
Fusion gene informationFusion gene name: SETD2-MRPL44
Fusion gene ID: 80317
HgeneTgene
Gene symbol

SETD2

MRPL44

Gene ID

29072

65080

Gene nameSET domain containing 2, histone lysine methyltransferasemitochondrial ribosomal protein L44
SynonymsHBP231|HIF-1|HIP-1|HSPC069|HYPB|KMT3A|LLS|SET2|p231HBPCOXPD16|L44MT|MRP-L44
Cytomap

3p21.31

2q36.1

Type of geneprotein-codingprotein-coding
Descriptionhistone-lysine N-methyltransferase SETD2SET domain containing 2huntingtin interacting protein 1huntingtin yeast partner Bhuntingtin-interacting protein Blysine N-methyltransferase 3Aprotein-lysine N-methyltransferase SETD239S ribosomal protein L44, mitochondrialmitochondrial large ribosomal subunit protein mL44
Modification date2020031520200313
UniProtAcc.

Q9H9J2

Ensembl transtripts involved in fusion geneENST00000409792, ENST00000492397, 
ENST00000258383, 
Fusion gene scores* DoF score27 X 19 X 16=82081 X 2 X 1=2
# samples 412
** MAII scorelog2(41/8208*10)=-4.32333491610161
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/2*10)=3.32192809488736
Context

PubMed: SETD2 [Title/Abstract] AND MRPL44 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSETD2(47205344)-MRPL44(224824251), # samples:2
Anticipated loss of major functional domain due to fusion event.SETD2-MRPL44 seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
SETD2-MRPL44 seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
SETD2-MRPL44 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
SETD2-MRPL44 seems lost the major protein functional domain in Hgene partner, which is a IUPHAR drug target due to the frame-shifted ORF.
SETD2-MRPL44 seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
SETD2-MRPL44 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneSETD2

GO:0010569

regulation of double-strand break repair via homologous recombination

24843002

HgeneSETD2

GO:0018023

peptidyl-lysine trimethylation

27518565

HgeneSETD2

GO:0018026

peptidyl-lysine monomethylation

28753426

HgeneSETD2

GO:0032465

regulation of cytokinesis

27518565

HgeneSETD2

GO:0032727

positive regulation of interferon-alpha production

28753426

HgeneSETD2

GO:0034340

response to type I interferon

28753426

HgeneSETD2

GO:0051607

defense response to virus

28753426

HgeneSETD2

GO:0097198

histone H3-K36 trimethylation

23043551|24843002|26002201|27474439|28753426

HgeneSETD2

GO:0097676

histone H3-K36 dimethylation

26002201

HgeneSETD2

GO:1902850

microtubule cytoskeleton organization involved in mitosis

27518565

HgeneSETD2

GO:1905634

regulation of protein localization to chromatin

24843002


check buttonFusion gene breakpoints across SETD2 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across MRPL44 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4OVTCGA-30-1861-01ASETD2chr3

47205344

-MRPL44chr2

224824251

+
ChimerDB4OVTCGA-30-1861SETD2chr3

47205343

-MRPL44chr2

224824250

+
ChimerDB4OVTCGA-30-1861-01ASETD2chr3

47205344

-MRPL44chr2

224824251

+


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Fusion Gene ORF analysis for SETD2-MRPL44

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
Frame-shiftENST00000409792ENST00000258383SETD2chr3

47205344

-MRPL44chr2

224824251

+
intron-3CDSENST00000492397ENST00000258383SETD2chr3

47205344

-MRPL44chr2

224824251

+
Frame-shiftENST00000409792ENST00000258383SETD2chr3

47205343

-MRPL44chr2

224824250

+
intron-3CDSENST00000492397ENST00000258383SETD2chr3

47205343

-MRPL44chr2

224824250

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for SETD2-MRPL44


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)
SETD2chr347205343-MRPL44chr2224824250+4.34E-101
SETD2chr347205343-MRPL44chr2224824250+4.34E-101
SETD2chr347205343-MRPL44chr2224824250+4.34E-101
SETD2chr347205343-MRPL44chr2224824250+4.34E-101

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for SETD2-MRPL44


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.MRPL44

Q9H9J2

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Component of the 39S subunit of mitochondrial ribosome. May have a function in the assembly/stability of nascent mitochondrial polypeptides exiting the ribosome. {ECO:0000269|PubMed:23315540}.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page


* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for SETD2-MRPL44


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for SETD2-MRPL44


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for SETD2-MRPL44


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for SETD2-MRPL44


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSETD2C0279702Conventional (Clear Cell) Renal Cell Carcinoma6CGI;CTD_human;UNIPROT
HgeneSETD2C4085873LUSCAN-LUMISH SYNDROME4CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneSETD2C0007134Renal Cell Carcinoma2CTD_human
HgeneSETD2C0023467Leukemia, Myelocytic, Acute2UNIPROT
HgeneSETD2C1266042Chromophobe Renal Cell Carcinoma2CTD_human
HgeneSETD2C1266043Sarcomatoid Renal Cell Carcinoma2CTD_human
HgeneSETD2C1266044Collecting Duct Carcinoma of the Kidney2CTD_human
HgeneSETD2C1306837Papillary Renal Cell Carcinoma2CTD_human
HgeneSETD2C1961102Precursor Cell Lymphoblastic Leukemia Lymphoma2UNIPROT
HgeneSETD2C0006142Malignant neoplasm of breast1CTD_human
HgeneSETD2C0010606Adenoid Cystic Carcinoma1CTD_human
HgeneSETD2C0010701Phyllodes Tumor1CTD_human
HgeneSETD2C0023418leukemia1CTD_human
HgeneSETD2C0033578Prostatic Neoplasms1CTD_human
HgeneSETD2C0175695Sotos' syndrome1ORPHANET
HgeneSETD2C0206656Embryonal Rhabdomyosarcoma1CTD_human
HgeneSETD2C0345967Malignant mesothelioma1CTD_human
HgeneSETD2C0376358Malignant neoplasm of prostate1CTD_human
HgeneSETD2C0600066Malignant Cystosarcoma Phyllodes1CTD_human
HgeneSETD2C0678222Breast Carcinoma1CTD_human
HgeneSETD2C0920269Microsatellite Instability1CTD_human
HgeneSETD2C1257931Mammary Neoplasms, Human1CTD_human
HgeneSETD2C1458155Mammary Neoplasms1CTD_human
HgeneSETD2C1535926Neurodevelopmental Disorders1CTD_human
HgeneSETD2C1721098Replication Error Phenotype1CTD_human
HgeneSETD2C3714756Intellectual Disability1GENOMICS_ENGLAND
HgeneSETD2C4704874Mammary Carcinoma, Human1CTD_human
TgeneMRPL44C3809339COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 161CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT